Associated Papers
Biochemical, Clinical, and Genetic Characteristics of Mexican Patients with Primary Hypertriglyceridemia, Including the First Case of Hyperchylomicronemia Syndrome Due to GPIHBP1 Deficiency.
Rodríguez-Gutiérrez PG et al.
International Journal of Molecular Sciences, 2022
A novel homozygous variant in GPIHBP1: A case series of familial chylomicronemia syndrome from Colombia.
González AR et al.
Journal of Clinical Lipidology, 0
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